Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGAGCTAAGTTAGCTCTTTCTGGGA[C/T]CTTCTTTACTTCTCAGGAGACGCAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
ANKRD29 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
ANKRD29 - ankyrin repeat domain 29 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308238.1 | 869 | Missense Mutation | GAT,GGT | D,G 264 | NP_001295167.1 | |
NM_173505.3 | 869 | Missense Mutation | GAT,GGT | D,G 297 | NP_775776.2 | |
XM_011525830.2 | 869 | Missense Mutation | GAT,GGT | D,G 264 | XP_011524132.1 | |
XM_011525831.2 | 869 | Missense Mutation | GAT,GGT | D,G 255 | XP_011524133.1 | |
XM_011525832.2 | 869 | Missense Mutation | GAT,GGT | D,G 247 | XP_011524134.1 | |
XM_017025561.1 | 869 | Missense Mutation | GAT,GGT | D,G 231 | XP_016881050.1 |